Medication Adverse EffectsWhat is the population frequency of patient-reported AEs for each RA medication? What is the distribution of bother associated with AEs for each RA medication? What are patient-acceptable levels of AE frequency and bother for clinical trials and shared decision making in practice? How should information on medication side effects be collected in clinical practice?
|
Online Patient-Centered Research SurveysHow do we identify and enroll a representative sample of patients with definite RA using online, web-based platforms? Should investigators complement online surveys with clinic-based recruitment strategies to target male or older populations? What is the best approach to elicit medication AEs, such as electronic symptom diaries? What are the implications for patient education and shared decision making?
|